(1S,2S)-()-N-p-Tosyl-1,2-diphenylethylenediamine
98%
- Product Code: 69061
CAS:
167316-27-0
| Molecular Weight: | 366.48 g./mol | Molecular Formula: | C₂₁H₂₂SO₂N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03095684 | |
| Melting Point: | 128-131 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, enabling the production of enantiomerically pure compounds. Its application extends to the synthesis of complex organic molecules, where it helps control stereochemistry, ensuring the desired spatial arrangement of atoms. Additionally, it is employed in research settings to study and optimize catalytic processes, contributing to advancements in synthetic organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 125-131 |
| Purity (HPLC) | 98-100% |
| Specific Rotation [α]20/D (c=1, CHCl3) | 33-36 |
| Appearance | White to pale yellow crystal or powder |
| Infrared Spectrum | Conforms to Structure |
| Solubility in Hot Acetonitrile | almost transparent |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿400.00 |
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| 1.000 G | 10-20 days | ฿780.00 |
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| 5.000 G | 10-20 days | ฿3,880.00 |
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(1S,2S)-()-N-p-Tosyl-1,2-diphenylethylenediamine
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, enabling the production of enantiomerically pure compounds. Its application extends to the synthesis of complex organic molecules, where it helps control stereochemistry, ensuring the desired spatial arrangement of atoms. Additionally, it is employed in research settings to study and optimize catalytic processes, contributing to advancements in synthetic organic chemistry.
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